Engineering non-conventional yeast Rhodotorula toruloides for ergothioneine production

• Published in: Biotechnology for biofuels Vol. 17; no. 1; p. 65
• Main Authors: Liu, Ke, Xiang, Gedan, Li, Lekai, Liu, Tao, Ke, Jie, Xiong, Liangbin, Wei, Dongzhi, Wang, Fengqing
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 13.05.2024; BioMed Central; BMC
• Subjects: Biosynthesis; CRISPR; CRISPR-assisted Cre recombination; E coli; Environmental protection; Enzymes; Ergothioneine; Fermentation; Genes; Genetic engineering; Genome editing; Genomes; High-throughput screening; Histidine; Industrial applications; Industrial engineering; Manufacturing engineering; Metabolic engineering; Methods; Microorganisms; Mutants; Operating costs; Organisms; Physiology; Production costs; Production processes; Recombination; Rhodotorula toruloides; S-Adenosylmethionine; Sulfur; Sulphur; Yeast; Yeast fungi; Yeasts; China; Ergothioneine; High-throughput screening; Metabolic engineering; Rhodotorula toruloides; CRISPR-assisted Cre recombination
• ISSN: 2731-3654; 2731-3654; 1754-6834
• DOI: 10.1186/s13068-024-02516-2

Ergothioneine (EGT) is a distinctive sulfur-containing histidine derivative, which has been recognized as a high-value antioxidant and cytoprotectant, and has a wide range of applications in food, medical, and cosmetic fields. Currently, microbial fermentation is a promising method to produce EGT as its advantages of green environmental protection, mild fermentation condition, and low production cost. However, due to the low-efficiency biosynthetic process in numerous cell factories, it is still a challenge to realize the industrial biopreparation of EGT. The non-conventional yeast Rhodotorula toruloides is considered as a potential candidate for EGT production, thanks to its safety for animals and natural ability to synthesize EGT. Nevertheless, its synthesis efficiency of EGT deserves further improvement. In this study, out of five target wild-type R. toruloides strains, R. toruloides 2.1389 (RT1389) was found to accumulate the highest EGT production, which could reach 79.0 mg/L at the shake flask level on the 7th day. To achieve iterative genome editing in strain RT1389, CRISPR-assisted Cre recombination (CACR) method was established. Based on it, an EGT-overproducing strain RT1389-2 was constructed by integrating an additional copy of EGT biosynthetic core genes RtEGT1 and RtEGT2 into the genome, the EGT titer of which was 1.5-fold increase over RT1389. As the supply of S-adenosylmethionine was identified as a key factor determining EGT production in strain RT1389, subsequently, a series of gene modifications including S-adenosylmethionine rebalancing were integrated into the strain RT1389-2, and the resulting mutants were rapidly screened according to their EGT production titers with a high-throughput screening method based on ergothionase. As a result, an engineered strain named as RT1389-3 was selected with a production titer of 267.4 mg/L EGT after 168 h in a 50 mL modified fermentation medium. This study characterized the EGT production capacity of these engineered strains, and demonstrated that CACR and high-throughput screening method allowed rapid engineering of R. toruloides mutants with improved EGT production. Furthermore, this study provided an engineered RT1389-3 strain with remarkable EGT production performance, which had potential industrial application prospects.